Trainings and webinars

for professionals in the pharmaceutial and medical device industry.

We are a European based company offering trainings and webinars on regulatory affairs, regulatory compliance, quality assurance and business organisation in the pharmaceutical, food supplement and medical device industry.
Register for one of or current trainings or contact us for your individual training plan.
Book now!
Upcoming trainings
Date Training Type Location Booking
5.7. - 13.9.2018 A series of 6 webinars:
The New EU Medical Device Regulation
Webinar Online Details
17.9. - 18.9.2018 Regulatory Affairs Strategies Public training London, UK Details
10.10. - 11.10.2018 Challenges in Drug/Device Combination Products Public training London, UK Details
03.12.- 04.12.2018 A practical guide to Pharmacovigilance Public training Singapore Details
05.12.- 06.12.2018 Contract Manufacturing Agreements Public training Singapore Details
New! Project Management

Project Management

...for Regulatory Affairs Professionals. Ensure a smooth process and the highest quality in the pharmaceutical and medical device business.
Project management
New! Regulatory Affairs Strategies

Regulatory Affairs Strategies

Effective registration process, best practices for integrating regulatory requirements and advice on how to develop RA project teams and strategies.
Regulatory Affairs Strategies
Regulatory requirements

Regulatory requirements in the US

Equip your professionals with the basis of the regulatory requirements in the US - guidelines, legislation, variations submissions, the FDA & more.
Regulatory requirements
Labelling and packaging

Labelling and packaging in the EU

Equip your professionals with a complete technical understanding of the regulatory framework of labelling in the European Union.
Labelling and packaging